GUNA-ORAL

GUNA-ORAL is an FDA-registered drug product whose active ingredient is ACHILLEA MILLEFOLIUM - ACONITUM NAPELLUS - ARNICA MONTANA - ATROPA BELLADONNA - CALCIUM SULFIDE - COMFREY ROOT - ECHINACEA ANGUSTIFOLIA - ECHINACEA PURPUREA - HYPERICUM PERFORATUM - SUS SCROFA TOOTH - WITCH HAZEL -. It is labelled by Guna spa taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 17089-452, label effective 20181221. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

Across FDA labelling, products containing ACHILLEA MILLEFOLIUM - ACONITUM NAPELLUS - ARNICA MONTANA - ATROPA BELLADONNA - CALCIUM SULFIDE - COMFREY ROOT - ECHINACEA ANGUSTIFOLIA - ECHINACEA PURPUREA - HYPERICUM PERFORATUM - SUS SCROFA TOOTH - WITCH HAZEL - are most often described in connection with: directions rotate, upright position, spray onto, affected areas, mouth throat, gingiva needed. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Directions : Rotate the nebulizer to the upright position. Spray onto affected areas: mouth, throat or gingiva as needed.

DIRECTIONS Adults and children 12 years and older 2 sprays, 3-5 times per day Children between 12 years and 6 years of age 1 spray t, 3-5 times per day Children under 6 years ask a doctor

WARNINGS Stop use and ask doctor if symptoms persist more than 3 days. If pregnant or breast-feeding ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Contains ethyl alcohol 20%

What is GUNA-ORAL used for?
Directions : Rotate the nebulizer to the upright position. Spray onto affected areas: mouth, throat or gingiva as needed.

Who makes GUNA-ORAL?
Guna spa is the labeler of record for GUNA-ORAL.

What form does GUNA-ORAL come in?
administered by oral. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is GUNA-ORAL prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Has GUNA-ORAL been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.